Peter E. Maligres

Merck & Co., Inc., Rahway, NJ, USA (United States) — United States

Chemistry · Physical Sciences

30h-index2.9kcitations87works14.02yr avg
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Research Topics

Catalytic C–H Functionalization Methods(17), Catalytic Cross-Coupling Reactions(17), Synthesis and Catalytic Reactions(14), Sulfur-Based Synthesis Techniques(12), Asymmetric Hydrogenation and Catalysis(11)

Publications87 total

Total Synthesis of Enlicitide Decanoate
Journal of the American Chemical Society·2025· 28 cited
Selective Synthesis of <i>N</i><sup>6</sup>,3′,5′-Tripivaloyladenosine via Dynamic Kinetic Crystallization and Regioselective Preparation of Pivalated 2′-Deoxy-2′-fluoroarabinoadenosines
Organic Process Research & Development·2024
Manufacturing Process Development for Uprifosbuvir (MK-3682): A Green and Sustainable Process for Preparing Penultimate 2′-Deoxy-α-2′-Chloro-β-2′-Methyluridine
Organic Process Research & Development·2022· 1 cited
Diverse Catalytic Reactions for the Stereoselective Synthesis of Cyclic Dinucleotide MK-1454
Journal of the American Chemical Society·2022· 45 cited
Engineered Ribosyl-1-Kinase Enables Concise Synthesis of Molnupiravir, an Antiviral for COVID-19
ACS Central Science·2021· 181 citedOpen Access
Discovery and Development of an Unusual Organocatalyst for the Conversion of Thymidine to Furanoid Glycal
Organic Process Research & Development·2021· 6 cited
Organocatalytic Conversion of Nucleosides to Furanoid Glycals
The Journal of Organic Chemistry·2021· 10 cited
Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods
Chemical Science·2021· 21 citedOpen Access
Evolving to an Ideal Synthesis of Molnupiravir, an Investigational Treatment for COVID-19
2020· 6 citedOpen Access
Evolving to an Ideal Synthesis of Molnupiravir, an Investigational Treatment for COVID-19
2020· 35 citedOpen Access
Synthesis of Fused Oxepane HIV Integrase Inhibitor MK-1376
Synthesis·2020· 3 cited
CCDC 1876146: Experimental Crystal Structure Determination
The Cambridge Structural Database·2019Open Access
Preparation of 2-(2<i>H</i>-Tetrazol-2-yl)benzoic Acids via Regioselective Cu(I) Catalyzed N2 Arylation of Tetrazole
Organic Process Research & Development·2019· 6 cited
A multifunctional catalyst that stereoselectively assembles prodrugs
Science·2017· 181 cited
CCDC 1525797: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
CCDC 1523528: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
CCDC 1523527: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
CCDC 1523526: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
ChemInform Abstract: An Approach to Heterodiarylmethanes via sp<sup>2</sup>—sp<sup>3</sup> Suzuki—Miyaura Cross‐Coupling.
ChemInform·2016
A Robust Kilo-Scale Synthesis of Doravirine
Organic Process Research & Development·2016· 63 cited
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Frequent Co-authors

Shane W. Krska(12), Robert A. Reamer(10), David Askin(9), Guy R. Humphrey(8), Paul J. Reider(7), Sebastian Wendeborn(7), R. P. Volante(6), K. C. Nicolaou(6), Robert E. Maleczka(5), Milton R. Smith(5), Artis Klapars(5), Louis‐Charles Campeau(5), Sean Preshlock(4), Jongrock Kong(4), Deeptak Verma(4), Neil A. Strotman(4), Patrick S. Fier(4), Rebecca T. Ruck(4), Veena Upadhyay(4), Lushi Tan(4)